[PMID 19438904] Clinical associations of the genetic variants of CTLA-4, Tg, TSHR, PTPN22, PTPN12 and FCRL3 in patients with Graves' disease


[PMID 21040781] CTLA-4 confers a risk of recurrent schizophrenia, major depressive disorder and bipolar disorder in the Chinese Han population


[PMID 18773895] The genetic basis of primary biliary cirrhosis: premises, not promises.


[PMID 18778710] Primary biliary cirrhosis is associated with a genetic variant in the 3' flanking region of the CTLA4 gene.


[PMID 19300490] An African ancestry-specific allele of CTLA4 confers protection against rheumatoid arthritis in African Americans.


[PMID 19609446] CTLA4 autoimmunity-associated genotype contributes to severe pulmonary tuberculosis in an African population.


[PMID 19622768] CTLA4 variants, UV-induced tolerance, and risk of non-melanoma skin cancer.


[PMID 19672595] Polymorphisms in the CD28/CTLA4/ICOS genes: role in malignant melanoma susceptibility and prognosis?


[PMID 19956097] Remapping the type I diabetes association of the CTLA4 locus.


[PMID 19956101] Overview of the Rapid Response data.


[PMID 20352109] Association of the CTLA4 gene with Graves' disease in the Chinese Han population.


[PMID 22977635] Association study between polymorphisms of CD28, CTLA4 and ICOS and non-segmental vitiligo in a Korean population

rs231777

Parent Gene: CTLA4

Importance: 1
Less common allele: T = 14%
More common allele: C = 86%
My Genotype: Log In